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lumicain
lumicain - 10733-412-60 - (Aluminium Chloride Hexahydrate)
Drug Information of lumicain
| Product NDC: | 10733-412 |
| Proprietary Name: | lumicain |
| Non Proprietary Name: | Aluminium Chloride Hexahydrate |
| Active Ingredient(s): | 250 mg/g & nbsp; Aluminium Chloride Hexahydrate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of lumicain
| Product NDC: | 10733-412 |
| Labeler Name: | Medical Products Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100929 |
Package Information of lumicain
| Package NDC: | 10733-412-60 |
| Package Description: | 67 g in 1 BOTTLE (10733-412-60) |
NDC Information of lumicain
| NDC Code | 10733-412-60 |
| Proprietary Name | lumicain |
| Package Description | 67 g in 1 BOTTLE (10733-412-60) |
| Product NDC | 10733-412 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Aluminium Chloride Hexahydrate |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100929 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Medical Products Laboratories, Inc. |
| Substance Name | ALUMINUM CHLORIDE |
| Strength Number | 250 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
